A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001666



Internal ID19090883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77737747..77763491hg38UCSC Ensembl
Innerchr2:77964873..77990617hg19UCSC Ensembl
Innerchr2:77818381..77844125hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3825745
hg1925745
hg1825745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582062
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001666
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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